1. Volume 35, Issue 2, Pages 243-254 (July 2002)
Mice with Truncated MeCP2 Recapitulate Many Rett Syndrome Features and Display Hyperacetylation of Histone H3 
Mona D. Shahbazian, Juan I. Young, Lisa A. Yuva-Paylor, Corinne M. Spencer, Barbara A. Antalffy, Jeffrey L. Noebels, Dawna L. Armstrong, Richard Paylor, Huda Y. Zoghbi 
Neuron 
Volume 35, Issue 2, Pages (July 2002)
DOI: /S (02)

2. Figure 1 Generation of Mice that Produce a Truncated Version of MeCP2
(A) Strategy for targeting a premature stop codon (TAA) into the coding region of Mecp2. The stop codon was inserted along with a neomycin-resistance cassette immediately after the transcriptional repression domain.
(B) Southern blot of ES cell DNA, digested with EcoRV and hybridized with the 5′ and 3′ probes, reveals that the intended recombination event had occurred.
(C) The intact MeCP2 protein (74 kDa) is visible on a Western blot of extracts from transfected cells (POS) and wild-type (WT) mice, but not in mutant (MUT) mice, when probed with the MeCP2C17 antibody that recognizes amino acids 388–404. The MeCP2N15 antibody, which recognizes amino acids 164–178, detects full-length MeCP2 in extracts from transfected cells and wild-type mice but detects a truncated, 52 kDa protein in extracts from mutant mice.
(D) Staining of brain tissue with a carboxy-terminal (C-term) antibody confirms that intact MeCP2 is absent from mutant brain (CA3 region of the hippocampus is shown). The truncated protein, recognized by the MeCP2N15 antibody localizes normally to heterochromatic domains. The scale bar in (D) represents 25 μm and applies to all images in that panel.
Abbreviations: MBD, methyl-CpG binding domain; TRD, transcriptional repression domain; NLS, nuclear localization signal.
Neuron  , DOI: ( /S (02) )

3. Figure 2
Kyphosis and Spontaneous Myoclonic Seizures in Mecp2308/y Mice
(A) At ages over 7 months, Mecp2308/y mice (MUT) frequently developed kyphosis, whereas their wild-type littermates (WT) maintained a normal posture.
(B) Bilateral cortical discharges were evident during a spontaneous myoclonic seizure in an adult Mecp2 mutant mouse. Each spike-wave discharge was accompanied by a major myoclonic jerk involving the head and forelimbs. Normal behavior and EEG rhythms returned immediately following the discharge.
(C) Mutant mice displayed a normal EEG pattern during the interictal recording period. See supplemental movie S1 online for a video recording of the myoclonic episode.
Neuron  , DOI: ( /S (02) )

4. Figure 3
Mecp2308/y Mice Display a Progressive Decline in Motor Skills But Have Normal Strength
(A) Mutant mice (n = 10) performed similarly to wild-type (n = 12) on the accelerating rotating rod (rotarod) apparatus.
(B) When the rotarod apparatus was modified to remove the grips from the rod surface, mutant mice (n = 9) demonstrated an impaired ability to remain on the rod compared to wild-type (n = 12).
(C–E) Mutant mice (n = 24) were deficient in their ability to hold onto a pole that transitions from a horizontal to a vertical position and (D) to hang onto a thin, metal wire by their forepaws, as compared with wild-type (n = 19). Whereas wild-type mice (n = 6) remained on a wooden dowel for a maximum time of 2 min, Mecp2308/y mice tended to fall off (n = 7) (E).
(F) These deficits did not appear to be due to muscle weakness, as forepaw grip strength was normal.
(G) Although young males showed normal performance on the dowel, older males were impaired, and heterozygous females of the same older age were not.
(H) On the suspended wire, males were normal at 5–6 weeks of age but subsequently declined in performance at older ages.
(I) Heterozygous females suspended themselves as long as wild-type mice at 5–6 weeks of age, but not at 35–39 weeks.
Abbreviations: WT, wild-type; MUT, mutant; HET, heterozygous; FDx, forward direction on day x; BDx, backward direction on day x.
Neuron  , DOI: ( /S (02) )

5. Figure 4
Mecp2 Mutant Mice Are Less Active and Show Heightened Levels of Anxiety
(A–C) In the open-field test for locomotor activity, Mecp2308/y mice (n = 24) travel less distance and (B) spend less time moving, but (C) travel at a speed similar to wild-type (n = 19).
(D) Mutant mice also rear less than wild-type.
(E) Whereas wild-type mice increase their activity in the center of the open-field arena over time, mutant mice do not, suggesting that they may have increased anxiety.
Abbreviations: WT, wild-type; MUT, mutant.
Neuron  , DOI: ( /S (02) )

6. Figure 5
Abnormal Social Interactions between Wild-Type and Mecp2308/y Mice
(A) When wild-type (n = 9) and mutant (n = 9) mice faced one another in the tube test, wild-type mice retreated from the tube in a majority of cases.
(B) In the resident-intruder test, wild-type and mutant resident mice initiated the same number of various types of interactions during the 5 min testing period. Wild-type intruders, however, showed a decrease in the number of rear-sniffing events toward mutant mice.
(C) Wild-type and mutant residents interacted with intruders for the same amount of time during the testing period, but the total time of interactions initiated by intruders was decreased when the resident was a mutant.
Abbreviations: WT, wild-type; MUT, mutant.
Neuron  , DOI: ( /S (02) )

7. Figure 6
Mecp2 Mutant Mice Do Not Show Deficits in Two Learning and Memory Paradigms
(A) In a conditioned fear test, Mecp2 mutant mice (n = 24) learned as well as wild-type animals (n = 19) to associate an environment (context) and a conditioned stimulus (CS) with a foot shock, as measured by freezing behavior.
(B) In the Morris water task, the time to locate a submerged platform was similar in wild-type and mutant mice.
(C) The swimming speed of mutant mice was also comparable to wild-type.
(D and E) With the platform removed from the pool of water, wild-type and mutant mice searched the quadrant where the platform was previously located and crossed the exact position of the platform with equal frequency.
Abbreviations: WT, wild-type; MUT, mutant.
Neuron  , DOI: ( /S (02) )

8. Figure 7
Tissue-Specific Hyperacetylation of Histone H3 in Mecp2308/y Mice
Analysis of acid-extracted proteins revealed elevated levels of histone H3 acetylation in the cerebellum, spleen, and cortex of Mecp2 mutant mice. In nuclear extracts, no difference in H3 acetylation was detectable in the liver, a tissue with very low levels of MeCP2, whereas the difference was observed in the cortex. Between three and six mice of each genotype were independently analyzed for each tissue shown.
Abbreviations: WT, wild-type; MUT, mutant.
Neuron  , DOI: ( /S (02) )